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Nitric Acid
Muhammad Usama Akram
B1F17BSCH0078
Introduction
 Nitric acid is a strong mineral acid. It is a mono-basic acid.
 It is a strong oxidizing agent and can oxidize metals and
nonmetals easily.
 Nitric acid (HNO3) is a colorless liquid that is used in the
manufacture of inorganic and organic nitrates and nitro
compounds for fertilizers, dye intermediates, explosives, and
many different organic chemicals.
Properties
 HNO3 is usually a fuming liquid.
 It is freely miscible with water.
 It freezes to a snow white solid at -46 C.
 It is a colorless volatile liquid.
 It has a pungent smell.
 Its specific gravity at 15 C is 1.53.
Uses
 As a starting material in the manufacture of nitrogen
fertilizers such as ammonium nitrate & ammonium etc. Large
amounts are reacted with ammonia to yield ammonium
nitrate.
 As a nitrating agent in the preparation of explosives such as
TNT, ammonium picrate (Dunnite)
 It is commonly used in science laboratories at schools for
experimenting when specifically testing for chloride.
Manufacturing
Methods
 INDUSTRIALLY NITRIC ACID IS PREPARED BY
FOLLOWING 3 METHODS:
 CHILE SALTPETRE METHOD BY NANO3
 BRIKLAND EYDE’S METHOD BY USING AIR
 OSTWALD’S METHOD
OSTWALD’S METHOD
Principle
 NH3 is oxidized into NO by air at 800 C in presence of Pt
(Platinum)catalyst with 10% Rh content.
 Materials used:
 Ammonia gas
 Water
 Oxygen gas
PROCESS
 The conversion of ammonia into nitric acid in this process is
done through the following steps:
 Step1
 Oxidation of ammonia to nitric oxide
 Ammonia is oxidized by air in the presence of Pt catalyst at
800°C to give nitric oxide.
4NH3 + 5O2 ——–> 4NO + 6H2O
 Heat liberated maintains the temperature of the catalyst.
Cont.
 Step 2
 Oxidation of NO to NO2
 The nitric oxide is oxidized by air at temperature below
100°C, to give nitrogen dioxide (NO2)
2NO + O2 ——> 2NO2
Cont.
 Step 3
 Formation of nitric acid
 Nitrogen dioxide is then converted to nitric acid by absorbing
NO2 in water, in the presence of air.
3NO2 + H2O ——> 2HNO3 + NO
Hydrochloric Acid
Introduction
 Hydrochloric acid is a clear, colorless, highly pungent solution of
hydrogen chloride (HCl) in water.
 It is a highly corrosive, strong mineral acid with many industrial
uses. Hydrochloric acid is found naturally in gastric acid.
 As an monoprotic acid and one of the six common strong
mineral acids, it is the least likely to be subject to an oxidation-
reduction reaction.
Properties
 It is available in many different concentrations in water, thus
its exact physical properties (boiling point, melting point and
density) vary accordingly.
 The concentrated grade (fuming hydrochloric acid) is about
38% HCl in water.
 Industrial-grade HCl is about 30% to 35%, while the
commercial grade (muriatic acid) is between 20% and 32%.
Household cleaning solutions of HCl are typically 10% to
12%, but these still need further dilution before use.
Manufacturing
Methods
 Synthesis from elements (Burning Process)
 Organic By-product Synthesis.
 Metallic chlorides with Sulfuric acid.
 Waste Incineration.
 Thermal decomposition of hydrated heavy metals
Organic by-product Synthesis
 Hydrochloric acid is made during chlorination of organic products as
follows:
 RH₂+ Cl₂→RCl + HCl
 Hydrochloric acid is also made during fluorination of chlorinated organic
products to manufacture (hydro)chlorofluorocarbons as follows:
 RCl + HF →RF + HCl
 Where RCl stands for chloroform, trichloro ethane, etc and RF
stands for (hydro) chlorofluorocarbons
Waste Incineration.
 From incineration of chlorinated organic waste:
C4H6Cl2 + 5O2 → 4CO2 + 2H2O + 2HCl
 After leaving the chlorination process, the HCl-containing gas
stream proceeds to the absorption column, where concentrated
liquid HCl is produced by absorption of HCl vapors into a weak
solution of hydrochloric acid.
 The HCl-free chlorination gases are removed for further
processing. The liquid acid is then either sold or used elsewhere
in the plant. The final gas stream is sent to a scrubber to remove
the remaining HCl prior to venting.
Nitric Acid and Hydrochloric Acid Manufacturing Methods
Nitric Acid and Hydrochloric Acid Manufacturing Methods

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Nitric Acid and Hydrochloric Acid Manufacturing Methods

  • 1.
  • 2. Nitric Acid Muhammad Usama Akram B1F17BSCH0078
  • 3. Introduction  Nitric acid is a strong mineral acid. It is a mono-basic acid.  It is a strong oxidizing agent and can oxidize metals and nonmetals easily.  Nitric acid (HNO3) is a colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals.
  • 4. Properties  HNO3 is usually a fuming liquid.  It is freely miscible with water.  It freezes to a snow white solid at -46 C.  It is a colorless volatile liquid.  It has a pungent smell.  Its specific gravity at 15 C is 1.53.
  • 5. Uses  As a starting material in the manufacture of nitrogen fertilizers such as ammonium nitrate & ammonium etc. Large amounts are reacted with ammonia to yield ammonium nitrate.  As a nitrating agent in the preparation of explosives such as TNT, ammonium picrate (Dunnite)  It is commonly used in science laboratories at schools for experimenting when specifically testing for chloride.
  • 7. Methods  INDUSTRIALLY NITRIC ACID IS PREPARED BY FOLLOWING 3 METHODS:  CHILE SALTPETRE METHOD BY NANO3  BRIKLAND EYDE’S METHOD BY USING AIR  OSTWALD’S METHOD
  • 8. OSTWALD’S METHOD Principle  NH3 is oxidized into NO by air at 800 C in presence of Pt (Platinum)catalyst with 10% Rh content.  Materials used:  Ammonia gas  Water  Oxygen gas
  • 9. PROCESS  The conversion of ammonia into nitric acid in this process is done through the following steps:  Step1  Oxidation of ammonia to nitric oxide  Ammonia is oxidized by air in the presence of Pt catalyst at 800°C to give nitric oxide. 4NH3 + 5O2 ——–> 4NO + 6H2O  Heat liberated maintains the temperature of the catalyst.
  • 10. Cont.  Step 2  Oxidation of NO to NO2  The nitric oxide is oxidized by air at temperature below 100°C, to give nitrogen dioxide (NO2) 2NO + O2 ——> 2NO2
  • 11. Cont.  Step 3  Formation of nitric acid  Nitrogen dioxide is then converted to nitric acid by absorbing NO2 in water, in the presence of air. 3NO2 + H2O ——> 2HNO3 + NO
  • 12.
  • 14. Introduction  Hydrochloric acid is a clear, colorless, highly pungent solution of hydrogen chloride (HCl) in water.  It is a highly corrosive, strong mineral acid with many industrial uses. Hydrochloric acid is found naturally in gastric acid.  As an monoprotic acid and one of the six common strong mineral acids, it is the least likely to be subject to an oxidation- reduction reaction.
  • 15. Properties  It is available in many different concentrations in water, thus its exact physical properties (boiling point, melting point and density) vary accordingly.  The concentrated grade (fuming hydrochloric acid) is about 38% HCl in water.  Industrial-grade HCl is about 30% to 35%, while the commercial grade (muriatic acid) is between 20% and 32%. Household cleaning solutions of HCl are typically 10% to 12%, but these still need further dilution before use.
  • 17. Methods  Synthesis from elements (Burning Process)  Organic By-product Synthesis.  Metallic chlorides with Sulfuric acid.  Waste Incineration.  Thermal decomposition of hydrated heavy metals
  • 18. Organic by-product Synthesis  Hydrochloric acid is made during chlorination of organic products as follows:  RH₂+ Cl₂→RCl + HCl  Hydrochloric acid is also made during fluorination of chlorinated organic products to manufacture (hydro)chlorofluorocarbons as follows:  RCl + HF →RF + HCl  Where RCl stands for chloroform, trichloro ethane, etc and RF stands for (hydro) chlorofluorocarbons
  • 19.
  • 20. Waste Incineration.  From incineration of chlorinated organic waste: C4H6Cl2 + 5O2 → 4CO2 + 2H2O + 2HCl  After leaving the chlorination process, the HCl-containing gas stream proceeds to the absorption column, where concentrated liquid HCl is produced by absorption of HCl vapors into a weak solution of hydrochloric acid.  The HCl-free chlorination gases are removed for further processing. The liquid acid is then either sold or used elsewhere in the plant. The final gas stream is sent to a scrubber to remove the remaining HCl prior to venting.